OXALIS 5- oxalis montana leaf cream 
Uriel Pharmacy Inc.

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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Directions: FOR TOPICAL USE ONLY.

Apply to skin as needed. Under age 2: Consult a doctor.

Active Ingredient: Oxalis e pl. tota 3X

Inactive Ingredients: Distilled water, Stearic acid, Isopropyl myristate, Lavender oil, Cetyl alcohol, Polyoxyl 40 stearate, Stearyl alcohol, Xanthan gum, Potassium sorbate, Frankincense oil, Myrrh oil, Grapefruit seed extract

Use: Temporary relief of cramps.

KEEP OUT OF REACH OF CHILDREN.

Warnings: FOR EXTERNAL USE ONLY.
Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing, consult a doctor before use. Avoid contact with eyes. Do not use if safety seal is broken or missing. Natural ingredients may cause color and/or scent variation.

Questions? Call 866.642.2858
Made by with care by Uriel, East Troy, WI 53120
www.urielpharmacy.com

Product Label

OXALIS 5 
oxalis 5 cream
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:48951-7106
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXALIS MONTANA LEAF (UNII: U1W3U02EW0) (OXALIS MONTANA LEAF - UNII:U1W3U02EW0) OXALIS MONTANA LEAF 5 [hp_X]  in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
XANTHAN GUM (UNII: TTV12P4NEE)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
FRANKINCENSE OIL (UNII: 67ZYA5T02K)  
MYRRH OIL (UNII: H74221J5J4)  
CITRUS PARADISI SEED (UNII: 12F08874Y7)  
Product Characteristics
Color white Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:48951-7106-5 60 g in 1 TUBE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved homeopathic 09/01/2009
Labeler - Uriel Pharmacy Inc. (043471163)
Establishment
Name Address ID/FEI Business Operations
Uriel Pharmacy Inc. 043471163 manufacture(48951-7106)

Revised: 11/2013
Document Id: 5b673c35-c468-4dc2-9b5f-47b79a337f8a
Set id: c2b5262d-cb21-4c87-b9e5-2370bba14a3e
Version: 1
Effective Time: 20131113
 
Uriel Pharmacy Inc.